Evidence map›Paper›PMID 34783859›Full record

ArticleThe Journal of experimental medicine2022

Advances toward structure-based drug discovery for inflammasome targets.

Li Wang, Michael A Crackower, Hao Wu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 50% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Li WangVentus Therapeutics, Waltham, MA.
Michael A CrackowerVentus Therapeutics, Waltham, MA.
Hao WuDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA.
Boston Children's Hospital · US

Funding

NLRP1 and CARD8 Inflammasomes: Assembly, Regulation and Stress SensingR01AI124491 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI WU, HAO · 2016 to 2025
$5.1M
NIAID NIH HHS R01 AI124491NIH HHS
6 · The paper itself

Abstract

Inflammasome proteins play an important role in many diseases of high unmet need, making them attractive drug targets. However, drug discovery for inflammasome proteins has been challenging in part due to the difficulty in solving high-resolution structures using cryo-EM or crystallography. Recent advances in the structural biology of NLRP3 and NLRP1 have provided the first set of data that proves a promise for structure-based drug design for this important family of targets.

Indexed as

AnimalsCryoelectron MicroscopyDrug Delivery SystemsDrug DiscoveryHumansInflammasomesModels, MolecularMultiprotein ComplexesNLR Family, Pyrin Domain-Containing 3 ProteinNLR ProteinsPharmaceutical PreparationsProtein ConformationProtein MultimerizationSignal TransductionInflammasomesMultiprotein ComplexesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP1 protein, humanNLR ProteinsPharmaceutical Preparations

Identifiers

PMID34783859
PMCPMC8600719
OpenAlexW3212771708

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.